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The riddle of multinucleated “floret-like” giant cells and their detection in an extensive gluteal neurofibroma: a case report
INTRODUCTION: The neurofibromatoses are inherited tumor predisposition syndromes involving two major clinical phenotypes: neurofibromatosis type 1 (von Recklinghausen's disease) is linked to chromosome 17q, and tends to occur seven times more frequently than neurofibromatosis type 2. Neurofibro...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3751089/ https://ncbi.nlm.nih.gov/pubmed/23890233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-7-189 |
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